# FDA Inspection 977267 - Intelerad USA - June 29, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/intelerad-usa/f8dbeabe-433f-43da-be80-c8b6ba831c7b/
Source feed: FDA_Inspections

> FDA Inspection 977267 for Intelerad USA on June 29, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 977267
- Company Name: Intelerad USA
- Inspection Date: 2016-06-29
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 977267 - 2016-06-29](https://www.globalkeysolutions.net/api/records/fda_inspections/intelerad-usa/f80a9f7f-c4c9-45f6-92c8-b338ce5d1e98/)
- [FDA Inspection 832797 - 2013-05-22](https://www.globalkeysolutions.net/api/records/fda_inspections/intelerad-usa/38a1c886-00c1-414d-b80b-06e612dffd99/)
- [FDA Inspection 832797 - 2013-05-22](https://www.globalkeysolutions.net/api/records/fda_inspections/intelerad-usa/a842bf4d-3b21-4a27-8db7-88571bb43a7e/)

Company: https://www.globalkeysolutions.net/companies/intelerad-usa/1c4fae27-b3e8-4e97-be39-3216110cb8de

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7